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NCT06036446: LATCH

Cervical Cerclage for Short Cervix at 24-26 Weeks of Gestation: a Randomized Controlled Trial

Recruiting now NA Last updated 27 May 2026
What this trial tests

NA trial testing Cervical cerclage in Premature Birth in 329 participants. Currently enrolling.

Timeline
10 November 2023
Primary endpoint
1 October 2028
1 February 2029

Quick facts

Lead sponsorThomas Jefferson University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment329
Start date10 November 2023
Primary completion1 October 2028
Estimated completion1 February 2029
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Thomas Jefferson University

Who can join

Adults 18 to 50, female only, with Premature Birth. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The goal of this clinical trial is to determine whether cervical cerclage reduces the risk of preterm birth in patients with a short transvaginal ultrasound (TVU) cervical length (CL) ≤25mm between 24 0/7-26 6/7 weeks.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Cervical cerclage

Trials testing the same drug.

Other recruiting trials for Premature Birth

Currently open trials in the same condition.

Other Thomas Jefferson University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06036446.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing